Results 51 to 60 of about 138,022 (200)
Kikuchi-Fujimoto Disease Associated with Symptomatic CD4 Lymphocytopenia
Case Reports in Rheumatology, 2014 Kikuchi-Fujimoto disease is a rare benign condition of necrotising histiocytic lymphadenitis with unknown aetiology. We describe here a 30-year-old African American female who presented with fever, generalized rash, cervical lymphadenopathy, and oral ...
Meera Yogarajah, Bhradeev Sivasambu
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Kikuchi-Fujimoto Disease in a Filipino Boy: A Case Report
Philippine Journal of Otolaryngology Head and Neck Surgery, 2019 Objective: To report a case of a 12-year-old boy with Necrotizing Lymphadenitis (Kikuchi-Fujimoto disease) presenting as lymphadenitis secondary to multiple diagnosis.
Jenina Rachel Escalderon, Angelo Monroy
doaj +1 more source
A Case Report of Kikuchi-Fujimoto Disease with Immune Thrombocytopenic Purpura [PDF]
, 2010 Kikuchi-Fujimoto disease (histiocytic necrotizing lymphadenitis) is a rare disease characterized by lymphadenitis with fever. It is self-limited within one to four months, and is generally diagnosed by an excisional biopsy of the affected lymph node ...
강희철, 김원용, 이승범
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Zdravniški Vestnik, 2008 BACKGROUND The Kikuchi Fujimoto disease (KFD) or histiocytic necrotising lymphadenitis is a rarebenign disease, more common in Japanese women. In other parts of the world and also inEurope the disease in rare. The pathogenesis is poorly understood.Patients and methods We represent 2 patients who observed enlarged peripheral nodes, measuring up to2 cm ...
Marjana Glaser +2 more
+6 more sources
Optic Neuritis in a Pediatric Patient with Kikuchi-Fujimoto Disease: A Case Report and Review of the Literature. [PDF]
J Inflamm ResKikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a rare, benign, and self-limiting condition characterized by lymph node inflammation.
Bao S +11 more
europepmc +2 more sources
Recurrent Kikuchi-Fujimoto disease
BMJ Case Reports, 2010 We report the case of a 27-year-old, UK-born, Asian woman who suffered a rare recurrence of Kikuchi-Fujimoto disease. She presented with tender lymphadenopathy of the neck, fever and a prodrome of flu-like symptoms. She had a past medical history of biopsy-proven Kikuchi-Fujimoto disease of her right axilla 2 years earlier, which required no treatment.
Brendan Boyd, Spooner +3 more
openaire +3 more sources
Kikuchi Fujimoto lymphadenitis- an uncommon entity in the surgical outpatients: a case report [PDF]
, 2017 Kikuchi Fujimoto lymphadenitis is a benign self-limiting disease with subacute necrotizing lymphadenopathy of unknown cause. The clinical, histopathological and immunohistochemical features point to viral etiology hence delaying diagnosis commonly ...
Chougle, Qurratulain +4 more
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Kikuchi-Fujimoto Disease: A Rare Presentation in a Young Male. [PDF]
CureusKikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a rare benign condition characterized by cervical lymphadenopathy and constitutional symptoms mimicking tuberculosis.
Kedar AK +4 more
europepmc +2 more sources
Retinopathy in lupus transitioned to Kikuchi-Fujimoto disease
American Journal of Ophthalmology Case Reports, 2016 Purpose: We present a patient with systemic lupus erythematosus with significant vaso-occlusive retinal findings mimicking antiphospholipid antibody syndrome, who developed Kikuchi-Fujimoto disease.
Kelly S. Rue +2 more
doaj +1 more source
The significance of T-BET-positive CD8 T-cells with diminished CD5 expression in Kikuchi-Fujimoto disease. [PDF]
J Clin Exp HematopKikuchi-Fujimoto disease (KFD), also known as histiocytic necrotizing lymphadenitis, is a rare condition characterized by benign localized lymphadenopathy and clinical symptoms such as fever, sore throat, odynophagia, and leukopenia.
Yamashita T +11 more
europepmc +2 more sources